Asymmetric Synthesis of the Tricyclic Core of Calyciphylline A-Type Alkaloids via Intramolecular [3 + 2] Cycloaddition-Reference-Cited by-同舟云学术

Asymmetric Synthesis of the Tricyclic Core of Calyciphylline A-Type Alkaloids via Intramolecular [3 + 2] Cycloaddition

Published:2014-02-07 Issue:4 Volume:16 Page:1076-1079
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Lu¹,Xu Chen¹,Chen Li¹,Hao Xiaojiang²,Wang David Zhigang¹

Affiliation:

1. Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Shenzhen Graduate School of Peking University, Shenzhen 518055, China

2. Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650204, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol403609c

Reference41 articles.

1. The Daphniphyllum alkaloids

2. Paxiphyllines A and B, new alkaloids from Daphniphyllum paxianum

3. The isolation and structures of daphniteijsmine, daphnijsmine and desacetyldaphnijsmine

4. Calyciphyllines H–M, new Daphniphyllum alkaloids from Daphniphyllum calycinum

5. Synthesis of the 4-Azatricyclo[5.2.2.04,8]undecan-10-one Core of Daphniphyllum Alkaloid Calyciphylline A Using a Pd-Catalyzed Enolate Alkenylation

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